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Journal Abstract Search

130 related items for PubMed ID: 6107848

  • 21. Congenital heart disease in an infant with the Smith-Lemli-Opitz syndrome.
    Park SC, Needles CF, Dimich I, Sussman L.
    J Pediatr; 1968 Dec; 73(6):896-902. PubMed ID: 4386913
    [No Abstract] [Full Text] [Related]

  • 22. Ruvalcaba syndrome: autosomal dominant inheritance.
    Sugio Y, Kajii T.
    Am J Med Genet; 1984 Dec; 19(4):741-53. PubMed ID: 6517098
    [Abstract] [Full Text] [Related]

  • 23. Camptodactyly, genital abnormalities and mental retardation in four Indian boys.
    Suliman GI, Insley J, Rayner PH.
    Indian Pediatr; 1976 Apr; 13(4):311-4. PubMed ID: 939598
    [No Abstract] [Full Text] [Related]

  • 24. Japanese kindred with FG syndrome.
    Kato R, Niikawa N, Nagai T, Fukushima Y.
    Am J Med Genet; 1994 Aug 15; 52(2):242-3. PubMed ID: 7802020
    [No Abstract] [Full Text] [Related]

  • 25. Picture of the month.
    Stromquist C, Giacoia GP, Feingold M.
    Am J Dis Child; 1988 Sep 15; 142(9):981-2. PubMed ID: 3414632
    [No Abstract] [Full Text] [Related]

  • 26. [Noonan's syndrome].
    Guibaud P.
    Pediatrie; 1969 Mar 15; 24(2):221-4. PubMed ID: 4901597
    [No Abstract] [Full Text] [Related]

  • 27. [Aarskog syndrome (author's transl)].
    Kunze J, Spranger J.
    Klin Padiatr; 1973 Nov 15; 185(6):490-4. PubMed ID: 4798676
    [No Abstract] [Full Text] [Related]

  • 28. Autosomal dominant inheritance in Setleis syndrome.
    Masuno M, Imaizumi K, Makita Y, Nakamura M, Kuroki Y.
    Am J Med Genet; 1995 May 22; 57(1):57-60. PubMed ID: 7645599
    [Abstract] [Full Text] [Related]

  • 29. Aarskog syndrome: report of a family with review and discussion of nosology.
    Teebi AS, Rucquoi JK, Meyn MS.
    Am J Med Genet; 1993 Jun 15; 46(5):501-9. PubMed ID: 8322809
    [Abstract] [Full Text] [Related]

  • 30. Index finger hyperphalangy and multiple anomalies: Catel-Manzke syndrome?
    Wilson GN, King TE, Brookshire GS.
    Am J Med Genet; 1993 Apr 15; 46(2):176-9. PubMed ID: 8484405
    [Abstract] [Full Text] [Related]

  • 31. Aarskog-Scott syndrome: confirmation of linkage to the pericentromeric region of the X chromosome.
    Stevenson RE, May M, Arena JF, Millar EA, Scott CI, Schroer RJ, Simensen RJ, Lubs HA, Schwartz CE.
    Am J Med Genet; 1994 Sep 01; 52(3):339-45. PubMed ID: 7810566
    [Abstract] [Full Text] [Related]

  • 32. The Aarskog syndrome.
    Pedersen JC, Fryns JP, Bracke P, Geeraert M, Van der Berghe H.
    Ann Genet; 1980 Sep 01; 23(2):108-10. PubMed ID: 6967282
    [No Abstract] [Full Text] [Related]

  • 33. Syndromal foramina parietalia permagna: "new" or FG syndrome? Comments on the paper by Chrzanowska et al [1998].
    Rauch A, Opitz JM, Walker D.
    Am J Med Genet; 1998 Aug 06; 78(5):406-7. PubMed ID: 9714004
    [No Abstract] [Full Text] [Related]

  • 34. [Aarskog's syndrome (facial-digital-genital syndrome). Study of a family (author's transl)].
    Scarano G, Rinaldi MM, Cavaliere ML, Esposito M, Sicolo A, Santulli B, Stabile M, Fasano R, Ventruto V.
    Pediatr Med Chir; 1981 Aug 06; 3(4):323-5. PubMed ID: 7343926
    [Abstract] [Full Text] [Related]

  • 35. G--polysyndactyly in an Egyptian family.
    Temtamy SA, Lontly AH.
    Birth Defects Orig Artic Ser; 1974 Aug 06; 10(5):207-15. PubMed ID: 4469988
    [No Abstract] [Full Text] [Related]

  • 36. [Symphalangism (author's transl)].
    Szmurło J, Jakubowski K.
    Pol Przegl Radiol Med Nukl; 1979 Aug 06; 43(1):25-8. PubMed ID: 450741
    [No Abstract] [Full Text] [Related]

  • 37. [Anhidrotic ectodermal dysplasia (Christ-Siemens-Touraine-Syndrome) in an x-linked recessive mode of inheritance (author's transl)].
    Kuhlwein A, Weiss J.
    Dermatol Monatsschr; 1982 Jan 06; 168(1):34-43. PubMed ID: 7200917
    [No Abstract] [Full Text] [Related]

  • 38. New XLMR syndrome with characteristic face, hypogenitalism, congenital hypotonia and pachygyria.
    Zollino M, Mastroiacovo P, Zampino G, Mariotti P, Neri G.
    Am J Med Genet; 1982 Jan 06; 43(1-2):452-7. PubMed ID: 1605225
    [Abstract] [Full Text] [Related]

  • 39. IMAGe association: additional clinical features and evidence for recessive autosomal inheritance.
    Lienhardt A, Mas JC, Kalifa G, Chaussain JL, Tauber M.
    Horm Res; 2002 Jan 06; 57 Suppl 2():71-8. PubMed ID: 12065932
    [Abstract] [Full Text] [Related]

  • 40. Autosomal or X-linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy.
    Dahlberg PJ, Borer WZ, Newcomer KL, Yutuc WR.
    Am J Med Genet; 1983 Sep 06; 16(1):99-104. PubMed ID: 6638075
    [Abstract] [Full Text] [Related]

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